A Diels-Alder approach for the synthesis of highly functionalized benzo-annulated indane-based α-amino acid derivatives via a sultine intermediate
DSpace at IIT Bombay
View Archive InfoField | Value | |
Title |
A Diels-Alder approach for the synthesis of highly functionalized benzo-annulated indane-based α-amino acid derivatives via a sultine intermediate
|
|
Creator |
KOTHA, SAMBASIVARAO
GHOSH, ARUN KUMAR |
|
Subject |
cycloaddition
amino acids derivatives synthesis |
|
Description |
The synthesis of various highly functionalized benzo-annulated indane-based α-amino acid (AAA) derivatives are reported via a [4+2] cycloaddition strategy using a sultine derivative, containing an AAA moiety, as a reactive diene component. By adopting this strategy, a new α,α-dialkylated indane-based C60 fullerene containing a constrained AAA unit is reported.
|
|
Publisher |
Elsevier
|
|
Date |
2009-02-26T06:04:45Z
2011-11-25T17:29:59Z 2011-12-26T13:06:24Z 2011-12-27T05:54:14Z 2009-02-26T06:04:45Z 2011-11-25T17:29:59Z 2011-12-26T13:06:24Z 2011-12-27T05:54:14Z 2004 |
|
Type |
Article
|
|
Identifier |
Tetrahedron Letters 45(14), 2931-2934
0040-4039 http://dx.doi.org/10.1016/j.tetlet.2004.02.060 http://hdl.handle.net/10054/787 http://dspace.library.iitb.ac.in/xmlui/handle/10054/787 |
|
Language |
en
|
|